| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32394930dup | CA026178 | BRCA2 | c.9498dup (p.Glu3167Ter) c.*865dup (n.*865dup) c.9129dup (p.Glu3044Ter) c.*1060dup (n.*1060dup) c.*343dup (n.*343dup) c.9447dup (p.Glu3150Ter) c.1914dup (p.Glu639Ter) n.1625dup c.9506dup (n.9506dup) c.2376dup c.520dup (n.520dup) c.455dup c.9402dup (p.Glu3135Ter) | ClinVar dbSNP |
| 13 | g.32394930del | CA026179 | BRCA2 | c.9498del (p.Glu3167ArgfsTer15) c.*865del (n.*865del) c.9129del (p.Glu3044ArgfsTer?) c.*1060del (n.*1060del) c.*343del (n.*343del) c.9447del (p.Glu3150ArgfsTer?) c.1914del (p.Glu639ArgfsTer?) n.1625del c.9498del (p.Glu3167ArgfsTer?) c.9506del (n.9506del) c.2376del c.520del (n.520del) c.455del c.9402del (p.Glu3135ArgfsTer?) | ClinVar dbSNP |